The case for antihypertensive drug regimens that produce consistent 24-h bl
ood pressure control has largely been founded upon a series of epidemiologi
cal observations that were either cross-sectional or alternatively relative
ly small-scale followup studies. More recent data have unequivocally demons
trated, in a prospective study in hypertensive subjects with left ventricul
ar hypertrophy, that the reduction in left ventricular mass index during th
e course of one year's antihypertensive treatment, was predicted much more
closely by treatment-induced changes in ambulatory blood pressure than by c
hanges in clinic blood pressure. This provides definitive and confirmatory
data to support the aim of achieving blood pressure control, which is based
upon a smooth and consistent antihypertensive effect over a full 24-h dosa
ge interval. Regimens which provide such control may also offer the advanta
ge of a sustained duration of effect beyond 24 h. This characteristic is at
tractive because even the most compliant patient may inadvertently miss at
least one dose of medication each week. Evidence from a number of studies w
hich have sought to mimic this pattern of suboptimal compliance by delibera
tely inserting a placebo phase into a steady-state treatment regimen, has c
learly demonstrated the benefits of antihypertensive drugs with intrinsical
ly long duration of action. Furthermore, there is evidence to suggest that
following cessation of therapy there is a biphasic reversion of blood press
ure towards baseline levels with a maintenance of a residual effect which i
s more pronounced with a long-acting agent when compared to a shorter-actin
g dug from the same therapeutic class. There is increasing evidence, albeit
not derived from prospective outcome studies, that indicates that the bene
fits of antihypertensive therapy are likely to be maximized by treatment re
gimens which result in sustained blood pressure control.